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book (5)


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Neurodevelopmental disorders
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ISBN: 1280761075 9786610761074 0198028695 9780198028697 019512314X 9780195123142 019512314X 0190284145 Year: 1999 Publisher: New York Oxford University Press

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Abstract

This is a summary of a vast body of literature concerning diagnosis and treatment for a variety of neurodevelopmental disorders, including both common and rare conditions. All chapters have case studies to model treatment recommendations and appendices reviewing resources.


Book
Treatments of neurodevelopmental disorders
Authors: ---
ISBN: 0199378886 0199379874 0199937818 9780199937813 9780199937806 019993780X 1306877784 9781306877787 9780199379873 9780199380138 0199380139 9780199378883 Year: 2014 Publisher: New York, NY

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Abstract

This cutting-edge book brings advances in genetics, neurobiology, and psychopharmacology to the clinic to enhance treatment for neurodevelopmental disorders. Significant progress has been made in identifying the neurobiological mechanisms of several disorders and targeted treatments are modifying the outcome of these disorders. However, the ability to utilize this knowledge has not been summarized in one place for the practicing clinician. This book will fill that gap by providing the theoretical underpinnings and the latest advances in targeted treatments. Several neurodevelopmental disorders

The fragile X syndrome : diagnosis, biochemistry and intervention.
Authors: ---
ISBN: 0915667002 Year: 1983 Publisher: Oxnard Spectra

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Book
Fragile X syndrome and premutation disorders
Authors: ---
ISBN: 1911612395 1911612387 1911612409 9781911612377 9781911612407 9781911612384 9781911612391 1911612379 Year: 2020 Publisher: London

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Abstract

This book covers both molecular and clinical aspects of Fragile X Syndrome (FXS) and premutation disorders so that new targeted treatments can be understood by clinicians and parents. It covers all premutation disorders including FXTAS, FXPOI and FXAND problems. The main focus is to help clinicians to give the best care possible to patients with FXS and to understand a multidisciplinary treatment approach. Underserved populations such as babies and toddlers with FXS and mothers with the full mutation are highlighted, including the treatments that can be beneficial to them. This book also discuss fragile X associated disorders as they impact the family whose proband has FXS. A highlight of this book is the international perspective on how different cultures deal with FXS and targeted treatments.

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